Job Description
Join to apply for the Chemist, R&D Analytical role at SUN PHARMA
3 days ago Be among the first 25 applicants
Join to apply for the Chemist, R&D Analytical role at SUN PHARMA
Get AI-powered advice on this job and more exclusive features.
- Maintain the highest standards of scientific professionalism. When in doubt, get feedback from other R&D/Technical professionals.
- Maintain detailed and comprehensive documentation of all work performed.
- Stay current with the scientific literature, particularly in areas that may affect companys product line, existing processes or potential commercial opportunities.
- Evaluate technology packages from external sources for chemical and cost-effective viability, as directed.
- Perform literature searches for development work, potential projects, and to support QA/QC and Environmental/Health & Safety.
- Provide ideas for investigation with an emphasis on commercialization, patent opportunity, or publication on a regular basis.
- Provide support to QA/QC by writing analytical SOPs.
- Communicate results by providing timely reports and project updates, to include technical reports and summaries for company business units and customers.
- Provide monthly report on progress of work to the department head.
- Provide help on preparation of quarterly/yearly R&D summaries of ongoing work to peers and senior management.
- Plan and develop robust analytical methods including troubleshooting and validation, as appropriate.
- Work closely with Synthesis group and support on routine analysis.
- Work closely with Quality Assurance (QA) and Quality Control (QC) to identify project needs and to insure strict compliance with internal quality and/or cGMP/ICH guidelines.
- Work closely with QA on validation efforts for new API processes to insure strict cGMP compliance, where appropriate.
- Work closely with R&D team to answer DMF deficiencies and customer queries.
- Maintain rigorous accountability and documentation of work related to controlled substances in accordance with established SOPs and requirements of federal regulations (21 CFR Part 1300-1399).
- Adhere to all relevant company SOPs and guidelines, and provide input for correcting and changing existing procedures and processes.
- Provide technical support as needed for company products, analytical methods and customer-driven issues, as needed.
- Provide necessary information on cost-saving and time-saving alternatives to current analytical and laboratory practices whenever and wherever possible.
- Assist in supervision of R&D laboratory operations in general, including troubleshooting of lab systems and instrumentation.
- Work with Health, Safety and Environmental representative to identify waste stream data and possible hazards for potential products and processes.
- Assist in the maintenance and cleaning of the R&D laboratory in general and in individual workspace in particular.
- Seek out opportunities for professional development.
- Select and purchase R&D chemicals, glassware and supplies, and track these orders using the established R&D purchase requisition system.
- Execute R&D stability program, to include writing and following stability protocols, and packaging and testing APIs, as well as compiling and reporting stability results to R&D manager.
- Facilitate the training system within the R&D department in coordination with the requirements set forth by QA.
- Other duties as assigned.
Position Duties - Maintain the highest standards of scientific professionalism. When in doubt, get feedback from other R&D/Technical professionals.
- Maintain detailed and comprehensive documentation of all work performed.
- Stay current with the scientific literature, particularly in areas that may affect companys product line, existing processes or potential commercial opportunities.
- Evaluate technology packages from external sources for chemical and cost-effective viability, as directed.
- Perform literature searches for development work, potential projects, and to support QA/QC and Environmental/Health & Safety.
- Provide ideas for investigation with an emphasis on commercialization, patent opportunity, or publication on a regular basis.
- Provide support to QA/QC by writing analytical SOPs.
- Communicate results by providing timely reports and project updates, to include technical reports and summaries for company business units and customers.
- Provide monthly report on progress of work to the department head.
- Provide help on preparation of quarterly/yearly R&D summaries of ongoing work to peers and senior management.
- Plan and develop robust analytical methods including troubleshooting and validation, as appropriate.
- Work closely with Synthesis group and support on routine analysis.
- Work closely with Quality Assurance (QA) and Quality Control (QC) to identify project needs and to insure strict compliance with internal quality and/or cGMP/ICH guidelines.
- Work closely with QA on validation efforts for new API processes to insure strict cGMP compliance, where appropriate.
- Work closely with R&D team to answer DMF deficiencies and customer queries.
- Maintain rigorous accountability and documentation of work related to controlled substances in accordance with established SOPs and requirements of federal regulations (21 CFR Part 1300-1399).
- Adhere to all relevant company SOPs and guidelines, and provide input for correcting and changing existing procedures and processes.
- Provide technical support as needed for company products, analytical methods and customer-driven issues, as needed.
- Provide necessary information on cost-saving and time-saving alternatives to current analytical and laboratory practices whenever and wherever possible.
- Assist in supervision of R&D laboratory operations in general, including troubleshooting of lab systems and instrumentation.
- Work with Health, Safety and Environmental representative to identify waste stream data and possible hazards for potential products and processes.
- Assist in the maintenance and cleaning of the R&D laboratory in general and in individual workspace in particular.
- Seek out opportunities for professional development.
- Select and purchase R&D chemicals, glassware and supplies, and track these orders using the established R&D purchase requisition system.
- Execute R&D stability program, to include writing and following stability protocols, and packaging and testing APIs, as well as compiling and reporting stability results to R&D manager.
- Facilitate the training system within the R&D department in coordination with the requirements set forth by QA.
- Other duties as assigned.
Position Requirements - B.S. degree in Chemistry (preferable), Chemical Engineering, or related discipline.
- Ability and attitude to assume a leadership role and work in a productive technical team within an industrial research environment.
- Ability to communicate effectively through verbal, written, presentation and computer modes of expression.
- Ability to confidently represent company on technical matters to customers, senior management, and at scientific venues (conferences and publications).
Seniority level
Seniority level
Entry level
Employment type
Employment type
Full-time
Job function
Job function
Research, Analyst, and Information Technology -
Industries
Pharmaceutical Manufacturing
Referrals increase your chances of interviewing at SUN PHARMA by 2x
Get notified about new Chemist jobs in Chattanooga, TN .
Fort Oglethorpe, GA $29.95-$42.08 2 weeks ago
Chattanooga, TN $45,000.00-$75,000.00 2 weeks ago
Chattanooga, TN $29.95-$42.08 2 months ago
Chattanooga, TN $29.95-$42.08 2 months ago
Expert Topical-Products Formulation Development Scientist
Fort Oglethorpe, GA $29.95-$42.08 2 weeks ago
Laboratory Unit - Laboratory Technician - $1,891 per week
Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Job Tags
Full time,